Process of producing an anti-reflection optical article

ABSTRACT

An anti-reflection optical article which has an excellent anti-reflection properties, scratch resistance, impact resistance, flexibility, anti-static properties and weatherability, and which is easy to dye is disclosed. The anti-reflection optical article of the present invention comprises a transparent plastic substrate; a hard coat film formed on a surface of the substrate, the film having an index of refraction of not less than 1.52; and a fluorine-containing organopolysiloxane-based film with a thickness of 10 nm to 500 nm, which has an index of refraction lower than that of the hard coat film by not less than 0.02, and which is formed on the hard coat film.

This application is a divisional of copending application Ser. No.07/114,061 filed on Oct. 29, 1987 now U.S. Pat. No. 4,904,525.

BACKGROUND OF THE INVENTION

I. Field of the Invention

This invention relates to an anti-reflection optical article withexcellent scratch resistance, dyeability, impact resistance, chemicalresistance, flexibility and weatherability. The anti-reflection opticalarticle of the present invention is suitable for optics and, forexample, optical lenses such as lenses of spectacles and cameras.

II. Description of the Prior Art

When an object is seen through a transparent material, if reflected raysare strong and a reflected image is clear, vision is disturbed, and areflected image such as so-called ghosts or flares are formed to give anunpleasant feel to one's eyes. In the case of using a looking glass, thecontent cannot be clearly seen because of rays reflected from the glasssurface.

There is also a problem in that the optical articles have a tendency toattract dust. Since the attraction is due to an electrostatic forceretained by the optical article, the dust is hardly removed by simplywiping the optical article.

A number of measures have been proposed for preventing the reflection,and some of them are currently used. Obtaining an anti-reflection effectby applying a liquid composition to a transparent substrate isdisclosed, for example, in U.S. Pat. No. 4,361,598, Japanese PatentDisclosure (Kokai) Nos. 167448/83, 211701/83, 43601/83 and 49501/84.

However, the optical articles disclosed in Japanese Patent Disclosure(Kokai) Nos. 167448/83 and 211701/83 are made of glass, so that theycannot be dyed. Not only in view of the dyeability, but also in view ofthe lightness, flexibility and processability, plastic substrates aredesired.

Optical articles having a plastic substrate are disclosed, for example,in U.S. Pat. No. 4,590,117 and Japanese Patent Disclosure (Kokai) Nos.43601/83 and 49501/84. However, those disclosed in these referencesemploy a structure including two or more layers, so that theproductivity, reproducibility and uniformity of the plane are not good.

It is also known that a fluorine-containing organopolysiloxane-basedthin film formed on the surface of an optical article for preventing thereflection (Japanese Patent Disclosure (Kokai) No. 40845/85).

On the other hand, for the prevention of attachment of dust to theoptical article, charging-preventing agents comprising a surface activeagent, which are to be applied to the optical article, are commerciallyavailable. However these agents show their effect only temporarily.

As to the prevention of the charging of the plastic mold articles,various methods are known such as, for example, those disclosed inJapanese Patent Publication (Kokoku) Nos. 15494/80 and 21628/85.

SUMMARY OF THE INVENTION

The object of the present invention is to provide an anti-reflectionoptical article having excellent anti-reflection properties, scratchresistance, dyeability, impact resistance, chemical resistance,flexibility and weatherability.

The above object and other objects of the present invention may beaccomplished by providing an anti-reflection optical article comprisinga transparent plastic substrate; a hard coat film formed on a surface ofthe substrate, the film having an index of refraction of not less than1.52; and a fluorine-containing organopolysiloxane-based film with athickness of 10 nm to 500 nm, which has an index of refraction lowerthan that of the hard coat film by not less than 0.02, and which isformed on the hard coat film.

This invention further provides a process of producing theabove-described anti-reflection optical article, comprising the steps ofproviding the transparent plastic substrate on which the hard coat filmhaving an index of refraction of not less than 1.52 is formed; applyinga liquid coating composition comprising a fluorine-containing organicsilicon compound and/or a hydrolysate thereof, on the hard coat film;and curing the applied composition to form the fluorine-containingorganopolysiloxane-based film with an index of refraction lower thanthat of the hard coat film by not less than 0.02.

The anti-reflection optical article of the present invention has anexcellent anti-reflection property, and a uniform reflection color maybe imparted. Since the surface of the optical article of the presentinvention is hard, it has an excellent scratch resistance, impactresistance and durability. The optical article of the present inventionmay be easily dyed and the dying speed is high. Further, the outerappearance after dying is nice. The surface of the optical article ofthe present invention is smooth, so that it is hardly scratched.

DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS

As stated above, the anti-reflection optical article of the presentinvention includes a transparent plastic substrate. Any plastic may beused for forming the substrate. Preferred examples of the plastics whichmay be used for forming the substrate include acrylic resins,polystyrenes, polycarbonates, diethyleneglycolbisallylcarbonatepolymers, di-(meta)-methacrylate polymers of (halogenated)bisphenol Aand copolymers thereof, urethane-modified (meta)acrylate polymers of(halogenated)bisphenol A and copolymers thereof.

A hard coat film is formed on a surface of the substrate. The term "hardcoat film" used herein used means a film having a pencil hardness of 4Hor more as determined by the method according to JIS K5400.

The hard coat film has an index of refraction of not less than 1.52. Ifthe index of refraction is less than 1.52, the anti-reflection propertymay not be obtained. In view of further promoting the anti-reflectionproperty, it is preferred that the index of refraction of the hard coatfilm be not less than 1.54.

Any material may be used for forming the hard coat film as long as ithas a pencil hardness of not less than 4H and an index of refraction ofnot less than 1.52. Preferred examples of the materials which may beused for forming the hard coat film may include organic resins such asacrylic resin, polyester resin, organopolysiloxane resin, polyurethane,cellulose derivatives, epoxide polymer, nylon resin, melamine resin andinorganic compounds such as inorganic oxides such as titanium oxide andzirconium oxide obtained from metal alkoxide or metal chelate.

It should be noted, however, in view of further increasing the surfacehardness and further promoting the adhesion with the fluorine-containingorganopolysiloxane-based film, and in view of the feasibility to givethe high index of refraction, it is preferred that the hard coat filmcontain inorganic microparticles having a high index of refraction.

Preferred exmaples of the microparticles to be contained in the hardcoat film may include microparticles of oxides of metals such astantalum, aluminum, titanium, zirconium, tin and antimony. These oxidesare preferred since they not only give a high index of refraction, butalso give a great hardness and high transparency. Among theabove-mentioned oxides, oxides of tantalum, zirconium, titanium andantimony are especially preferred in view of their stability. Thesemicroparticles may be used individually or in combination. The oxide maybe a composite oxide containing silicon or the like.

The inorganic microparticles preferably have a mean particle size ofabout 1-300 nm, more preferably about 5-200 nm, in view of not degradingthe transparency of the hard coat film.

If the content of the inorganic microparticles is too small, the effectof the microparticles may not be shown, and if its content is too great,the hard coat film may have a tendency to be cracked. Therefore, thecontent of the inorganic microparticles in the-hard coat film ispreferably 10-75% by weight, and more preferably 15-60% by weight.

The thickness of the hard coat film varies depending on the plasticmaterial forming the transparent substrate and should be selected tohave a pencil hardness of not less than 4H. If the hard coat film is toothin, it is difficult to obtain a sufficient hardness and a sufficientdyeability, and if the hard coat film is too thick, it is difficult toobtain a uniform film and the impact resistance may be degraded. Thus,the thickness of the hard coat film is usually 0.5 μm to 20 μm.

The hard coat film may be formed on the substrate by applying a liquidcoating composition comprising the above-described resin on the plastictransparent substrate and by curing the applied composition.

A fluorine-containing organopolysiloxane-based film (hereinafterreferred to as "top film" for short) with a thickness of 10-500 nm andan index of refraction which is lower than that of the hard coat film by0.02 or more is formed on the hard coat film.

The thickness of the top film is 10 nm to 500 nm, preferably 50 nm to300 nm. If the thickness of the top film is smaller than 10 nm,sufficient anti-reflection properties and a sufficient surface hardnessmay not be obtained. If the thickness of the top film is greater than500 nm, and anti-reflection effect may not be obtained.

The preferred top film is one obtained by applying to the hard coat filma liquid composition comprising a fluorine-containing organic siliconcompound of the formula (I) or a hydrolysate thereof:

    (R.sup.1 Q)SiX.sub.a Y.sub.3-a                             (I)

wherein R¹ is a C₁ -C₂₀ fluorine-containing alkyl group which maycontain one or more ether bonds and/or ester bonds; Q is a divalentorganic group; X is a C₁ -C₄ alkyl group; Y is a halogen, alkoxy orRCOO⁻ group (wherein R is hydrogen or a C₁ -C₄ alkyl group); and a is aninteger of 0 or 1.

Preferred examples of the fluorine-containing compound of the formula(I) may include 3,3,3-trifluoropropyltrialkoxysilane,3,3,3-trifluoropropylmethyldialkoxysilane and3-trifluoroacetoxypropyltrialkoxysilane.

It is preferred that the compound expressed by the formula (I) becontained in the top film in the amount of at least 10% by weight or incases where the index of refraction of the hard coat film is not sohigh, in the amount of at least 15% by weight.

To further improve the abrasion resistance, scratch resistance, impactresistance, chemical resistance, flexibility, light resistance andweatherability of the combination of the hard coat film and the topfilm, it is preferred that one or more of organic silicon compounds ofthe formula (II) be contained in the top film along with theabove-described fluorine-containing organopolysiloxane of the formula(I):

    R.sup.3.sub.b R.sup.4.sub.c SiZ.sub.4-(b+c)                (II)

wherein R³ and R⁴ are independently alkyl, alkenyl or aryl group or ahydrocarbon group containing halogen, epoxy, glycidoxy, amino, mercapto,methacryloxy or cyano group; Z is a hydrolyzable group; and b and cindependently mean 1 or 0.

Preferred examples of the compounds represented by the formula (II) mayinclude tetraalkoxysilanes such as methyl silicate, ethyl silicate,n-propyl silicate, i-propyl silicate, n-butyl silicate, sec-butylsilicate and t-butyl silicate and hydrolysates thereof;

trialkoxysilanes, triacyloxysilanes and triphenoxysilanes

such as methyltrimethoxysilane, methyltriethoxysilane,

methyltrimethoxyethoxysilane, methyltriacetoxysilane,

methyltripropoxysilane, methyltributoxysilane,

ethyltrimethoxysilane, ethyltriethoxysilane,

vinyltrimethoxysilane, vinyltriethoxysilane,

vinyltriacetoxysilane, vinyltrimethoxyethoxysilane,

phenyltrimethoxysilane, phenyltriethoxysilane,

phenyltriacetoxysilane, γ-chloropropyltrimethoxysilane,

γ-chloropropyltriethoxysilane,

γ-chloropropyltriacetoxysilane,

γ-methacryloxypropyltrimethoxysilane,

γ-aminopropyltrimethoxysilane,

γ-aminopropyltriethoxysilane,

γ-mercaptopropyltrimethoxysilane,

γ-mercaptopropyltriethoxysilane,N-β-(aminoethyl)-γ-aminopropyltrimethoxysilane,

β-cyanoethyltriethoxysilane, methyltriphenoxysilane,

chloromethyltrimethoxysilane,

chloromethyltriethoxysilane,

glycidoxymethyltrimethoxysilane,

glycidoxymethyltriethoxysilane,

α-glycidoxyethyltrimethoxysilane,

α-glycidoxyethyltriethoxysilane,

β-glycidoxyethyltrimethoxysilane,

β-glycidoxyethyltriethoxysilane,

α-glycidoxypropyltrimethoxysilane,

α-glycidoxypropyltriethoxysilane,

β-glycidoxypropyltrimethoxysilane,

β-glycidoxypropyltriethoxysilane,

γ-glycidoxypropyltrimethoxysilane,

γ-glycidoxypropyltriethoxysilane,

γ-glycidoxypropyltripropoxysilane,

γ-glycidoxypropyltributoxysilane,

γ-glycidoxypropyltrimethoxyethoxysilane,

γ-glycidoxypropyltriphenoxysilane,

α-glycidoxybutyltrimethoxysilane,

α-glycidoxybutyltriethoxysilane,

β-glycidoxybutyltrimethoxysilane,

β-glycidoxybutyltriethoxysilane,

γ-glycidoxybutyltriemthoxysilane,

γ-glycidoxybutyltriethoxysilane,

δ-glycicdoxybutyltrimethoxysilane,

δ-glycidoxybutyltriethoxysilane,

(3,4-epoxycyclohexyl)methyltrimethoxysilane,

(3,4-epoxycyclohexyl)methyltriethoxysilane,

β-(3,4-epoxycyclohexyl)ethyltrimethoxysilane,

β-(3,4-epoxycyclohexyl)ethyltriethoxysilane,

β-(3,4-epoxycyclohexyl)ethyltripropoxysilane,

β-(3,4-epoxycyclohexyl)ethyltributoxysilane,

β-(3,4-epoxycyclohexyl)ethyltrimethoxyethoxysilane,

β-(3,4-epoxycyclohexyl)ethyltriphenoxysilane,

γ-(3,4-epoxycyclohexyl)propyltrimethoxysilane,

γ-(3,4-epoxycyclohexyl)propyltriethoxysilane,

δ-(3,4-epoxycyclohexyl)butyltrimethoxysilane and

δ-(3,4-epoxycyclohexyl)butyltriethoxysilane as well as

hydrolysates thereof; and dialkoxysilanes,

diphenoxysilanes and diacyloxysilanes such as

dimethyldiemthoxysilane, phenylmethyldiemthoxysilane,

dimethyldiethoxysilane, phenylmethyldiethoxysilane,

γ-chloropropylmethyldimethoxysilane,

γ-chloropropylmethyldiethoxysilane,

dimethyldiacetoxysilane,

γ-methacryloxypropylmethyldimethoxysilane,

γ-methacryloxypropylmethyldiethoxysilane,

γ-mercaptopropylmethyldimethoxysilane,

γ-mercaptopropylmethyldiethoxysilane,

γ-aminopropylmethyldimethoxysilane,

γ-aminopropylmethyldiethoxysilane,

methylvinyldimethoxysilane, methylvinyldiethoxysilane,

glycidoxymethylmethyldimethoxysilane,

glycidoxymethylmethyldiethoxysilane,

α-glycidoxyethylmethyldimethoxysilane,

α-glycidoxyethylmethyldiethoxysilane,

β-glycidoxyethylmethyldimethoxysilane,

β-glycidoxyethylmethyldiethoxysilane,

α-glycidoxypropylmethyldimethoxysilane,

α-glycidoxypropylmethyldiethoxysilane,

β-glycidoxypropylmethyldiemthoxysilane,

β-glycidoxypropylmethyldiethoxysilane,

γ-glycidoxypropylmethyldimethoxysilane,

γ-glycidoxypropylmethyldiethoxysilane,

γ-glycidoxypropylmethyldipropoxysilane,

γ-glycidoxypropylmethyldibutoxysilane,

γ-glycidoxypropylmethyldimethoxyethoxysilane,

γ-glycidoxypropylmethyldiphenoxysilane,

γ-glycidoxypropylmethyldiacetoxysilane,

γ-glycidoxypropylethyldiethoxysilane,

γ-glycidoxypropylvinyldimethoxysilane,

γ-glycidoxypropylvinyldiethoxysilane,

γ-glycidoxypropylphenyldimethoxysilane and

γ-glycidoxypropylphenyldiethoxysilane, as well as hydrolysates thereof.

For the purpose of imparting dyeability, the organic silicon compoundshaving an epoxy group or a glycidoxy group are preferred.

To lower the curing temperature and to promote the curing, it ispreferred that the fluorine-containing organic silicon compound of theformula (I) or the mixture of the fluorine-containing silicon compoundand the organic silicon compound of the formula (II) be use after beinghydrolyzed.

Hydrolysis may be conducted by adding pure water or an aqueous solutionof an acid such as hydrochloric acid, acetic acid and sulfuric acid tothe organic silicon compound and by stirring the resulting mixture. Bycontrolling the amount of the water or the aqueous acid solution to beadded, the degree of hydrolysis may easily be controlled. In view of thepromotion of the curing, it is preferred that the water or the aqueousacid solution be added in the amount of not less than the equimolar ofthe -Y group in the formula (I) and not more than three times of themole number of the -Y group.

Although the hydrolysis may be conducted without using a solvent becausealcohols and the like are generated, for the purpose of conducting thehydrolysis uniformly, the hydrolysis may be conducted after mixing theorganic silicon compounds with a solvent. Further, it is possible topartly remove the alcohols and the like by heating and/or by reducedpressure, and it is also possible to add an appropriate solvent after aportion of the alcohols and the like are removed.

Preferred examples of the solvent may include alcohols such as ethanol,esters such as butyl acetate, ethers such as diethylether, dioxane,ketones such as methyl-isobutyl ketone, halogenated hydrocarbons such as1,1,2-trichloroethane, and aromatic hydrocarbons such as toluene andxylene. Those solvents may be used individually or in combination. Topromote the hydrolysis reaction, the mixture may be heated to atemperature higher than room temperature. In contrast, the mixture maybe cooled to a temperature lower than room temperature in order toconduct the hydrolysis reaction without causing preliminarypolymerization.

When applying the hard coat film on the plastic transparent substrate,or when applying the top film on the hard coat film, the surface of thetransparent substrate or the hard coat film is preferred to be subjectedto a pretreatment for the purpose of cleaning the surface, promoting theadhesivity, and promoting water resistance. Effective pretreatment mayinclude activated gas treatment and chemical treatment.

Activated gas treatment means a treatment with ions, electrons orexcited gas which are generated under the normal pressure or underreduced pressure. The activated gas may be generated by, for example,corona discharge and high voltage discharge by using direct electriccurrent, low frequency wave, high frequency wave or microwave underreduced pressure. The treatments with the low temperature plasmaobtained by high frequency wave discharge in reduced pressure and coronadischarge treatment are especially preferred.

Examples of the gas to be used herein may include oxygen, nitrogen,hydrogen, carbon dioxide, sulfur dioxide, helium, neon, argon, Freon(tradename of Du Pont), water vapor, ammonia, carbon monoxide, chlorine,nitrogen monoxide and nitrogen dioxide.

These gases may be used individually or in combination. In view ofimproving the adhesivity, a gas containing oxygen is preferred and airmay be used advantageously. Pure oxygen gas is still more preferred. Forthe purpose of improving the adhesivity, the activated gas treatment maybe conducted at an elevated temperature.

On the other hand, examples of the chemical treatment may include analkali treatment such as by sodium hydroxide, acid treatment such as byhydrochloric acid, sulfuric acid, potassium permanganate and potassiumdichromate, and treatment with an organic solvent having an aromaticring.

The above pretreatments may be conducted in combination continuously orstepwise.

For the curing of the liquid composition for forming the hard coat filmor the top film, a curing agent may be used to promote the curing andenabling the curing to be conducted under a low temperature. As thecuring agent, various curing agents for epoxy resins and various curingagents for organic silicon resins may be used.

Examples of the curing agents may include various organic acids and acidanhydrides thereof, nitrogen-containing organic compounds, various metalcomplexes, metal alkoxides, and various salts such as organiccarboxylates and carbonates of alkali metals. The curing agents may beused individually or in a combination.

Among these curing agents, in view of the stability of the compositionand coloring of the coated film, aluminum chelates represented by theformula (III) are especially preferred:

    AlX.sub.n Y.sub.3-n                                        (III)

wherein X is OL (L is a C₁ -C₄ alkyl); Y is a ligand selected from thegroup consisting of M¹ COCH₂ COM² (M¹ and M² are independently a C₁ -C₄alkyl) and M³ COCH₂ COOM⁴ (M³ and M⁴ are independently a C₁ -C₄ alkyl);n is 0, 1 or 2.

Among those represented by the formula (III), especially preferred arealuminum acetylacetonate, aluminumbisethylacetoacetatemonoacetylacetonate,aluminum-di-n-butoxide-monoethylaceto acetate andaluminum-di-iso-propoxide-monomethylaceto acetate, in view of thesolubility, stability and curing power as a curing agent. Thesecompounds may be used individually or in a combination.

To improve the flow of the applied composition, and to improve thesmoothness of the surface of the film to reduce the friction coefficientof the film surface, a surface active agent may be incorporated in thecomposition to be applied. Examples of the surface active agent mayinclude block or graft polymers of dimethylsiloxane and alkylene oxide;and fluorine-based surface active agents.

Dyes or pigments may be added to the composition for coloring the film.Further, fillers and organic polymers may be incorporated in thecomposition to improve the applicability of the composition, intimacy tothe substrate or film and to improve the physical properties of thefilm. Still further, to improve the weatherability, ultraviolet rayabsorbing agents may be contained in the composition. To improve theheat degration resistance, anti-oxidants may be contained in thecomposition.

To increase the surface hardness and to prevent the electric charging,silica sol of a large molecular weight silic acid anhydride in the formof a colloidal dispersion in water and/or an organic solvent such asethanol may preferably be added to the composition. In particular, whenthe silica sol is added to the top film, the abrasion resistance of thetop film is improved very much such that the top film may be resistantagainst the abrasion by Carborundum (tradename of Carborundum) powder.Preferred examples of the silicic acid may include colloidalsilica ofwhich average radius is 0.5-100 nm and which is acidic.

To promote the dyeability, various epoxy resins, melamine resins andnylon resins may be added to the composition.

The above-described additives may be added to the liquid composition inthe amount of, for example, 5 to 70 wt % based on dry weight.

When applying the coating composition, the composition may be dilutedwith a diluent for controlling the thickness of the applied coating andfor making the application operation easy. Preferred examples of thediluent may include water, alcohols such ethanol, esters such as butylacetate, ethers such as diethyleneglycoldimethyl ether, ketones such asmethyl-isobutyl ketone and halogenated hydrocarbons such as1,1,2-trichloroethane.

The reflectance of the surface of the optical article of the presentinvention, which surface requires anti-reflection property, is not morethan 2.7%. In cases in which the anti-reflection property is requiredfor both surfaces of the optical article, such as in the case of thelens of spectacles, the total reflectance of the both surfaces is notmore than 5.4%, i.e., the transmittance of the whole optical article isnot less than 94.6%.

In a preferred embodiment of the present invention, the electriccharging is reduced while keeping the anti-reflection property and otherexcellent properties of the above-described optical article of thepresent invention. In this embodiment, the average fluorine to siliconratio (F/Si) by weight in the entire top film is 0.02 to 10, and theratio in the uppermost region of the top film is less than 80% that ofthe entire top film. The term "uppermost region" herein means the regionfrom the surface to a depth of 1 nm to 30 nm from the surface. If thefluorine to silicon ratio is less than 0.02, anti-reflection propertymay be degraded, and if it is more than 10, the hardness of the top filmmay be reduced. If the fluorine to silicon ratio in the uppermost regionin the top film is not less than 80%, the prevention of electriccharging may not be accomplished.

This structure of the top film may be obtained by, for example,subjecting the top film to the above-mentioned activated gas treatment.The conditions of the activated gas treatment may be appropriatelyselected by those skilled in the art in view of the required anti-staticproperty.

It is also useful for preventing the electric charging to form on thetop film a second fluorine-containing organopolysiloxane-based filmhaving a F/Si ratio by weight of less than 80% that of the top layer. Byso doing, the same effect brought about by setting the F/Si ratio byweight in the uppermost region of the top layer to less than 80% may beobtained. The thickness of the second film is preferably 1 nm to 30 nmbecause a film thinner than 1 nm is difficult to prepare, and if thefilm is thicker than 30 nm, the anti-reflection property may bedegraded.

The second fluorine-containing organopolysiloxane film may be formed ina similar manner as in forming the top film, after chemical treatment ofthe top film. Examples of the chemical treatment may include treatmentswith alkali such as sodium hydroxide; with acid such as hydrochloricacid, sulfuric acid, potassium permanganate and potassium dichromate;and with organic solvent having an aromatic ring such as toluene,xylene, benzyl alcohol. The chemical treatment may be conductedindividually or in combination continuously or stepwise.

The fluorine/silicon weight ratio may be determined by a well-knownX-ray photoelectron analysis (ESCA).

Since the anti-reflection optical article of the present invention hasan excellent anti-reflection property, durable hard surface, dyeabilityand anti-static property, it is suited for use not only as a lens ofsunglasses and as an ophthalmic lens, but also as a camera lens and as abinocular lens.

The present invention will now be described by way of examples. Theexamples are presented for the purpose of illustration only, and theyshould not be interpreted as limiting the scope of the invention in anyway.

EXAMPLE 1, COMPARATIVE EXAMPLE 1 (1) Preparation of Transparent PlasticSubstrate

A transparent plastic substrate was obtained by cast polymerization of270 parts by weight of a polyfunctional acrylate monomer and 30 parts byweight of styrene using di-isopropylperoxide as an initiator, thepolyfunctional acrylate monomer having 0.9 mole ofhexamethylenediisocyanate per 1 mole of hydroxide group-containingcompound prepared by bonding via ester bond tetrabromobisphenol A having2 moles of ethylene oxide adduct with 1 mole of acrylic acid. The indexof refraction of the thus obtained resin was 1.61.

(2) Preparation of Coating Composition for Forming Hard Coat Film

(a) Preparation of Hydrolysate of γ-glycidoxypropyltrimethoxysilane

To a reactor with a rotating member of a magnetic stirrer, 95.3 g ofγ-glycidoxypropyltrimethoxysilane was fed. While keeping the temperatureof the liquid at 10° C., 21.8 g of 0.01 N aqueous hydrochloric acid wasadded dropwise while stirring the mixture with a magnetic stirrer. Afterfinishing the dropwise addition of the hydrochloric acid, cooling isstopped to obtain a hydrolysate of γ-glycidoxypropyltrimethoxysilane.

(b) Preparation of Coating Composition

To the thus obtained hydrolysate, were added 216 g of dimethylformamide,0.5 g of fluorine-based surface active agent and 67.5 g of bisphenol Atype epoxy resin (commercially available from Shell Chemical Co. underthe tradename of Epicoat 827), and the mixture was stirred. To themixture, were added 270 g of colloidal antimony pentaoxide sol (meanparticle size of 60 nm, commercially available from Nissan ChemicalIndustries, Ltd., Tokyo, Japan, under the tradename of Antimony SolA-2550) and 13.5 g of aluminum acetylacetonate, and then 1.1 g ofacetylacetone Cu(II) as a transition metal compound was added. Theresulting mixture was well stirred to obtain a coating composition forforming the hard coat film.

(3) Preparation of Coating Composition for Forming Fluorine-ContainingOrganopolysiloxane Film

(a) Preparation of Hydrolysate

To a reactor with a rotating member, 4.9 g of methyltrimethoxysilane and3.5 g of 3,3,3-trifluoropropyltrimethoxysilane were fed. While keepingthe temperature of the liquid at 10° C., 2.8 g of 0.01 N aqueoushydrochloric acid was added dropwise while stirring the mixture with amagnetic stirrer. After finishing the addition of the hydrochloric acid,cooling is stopped to obtain a hydrolysate.

(b) To the thus obtained hydrolysate, were added 56.0 g ofn-propylalcohol, 24.0 g of distilled water, 7.5 g of ethylCellosolve,1.0 g of silicone-based surface active agent in n-propylalcohol in aconcentration of 5% by weight, and 0.24 g of aluminum acetylacetonate.The mixture was well stirred to obtain a coating composition.

(4) Preparation of Anti-Reflection Optical Article

The transparent plastic substance obtained in (1) was coated with thecoating composition obtained in (2) by dipping the substrate in thecomposition. The thus coated lens was subjected to a preliminary curingat 110° C. for 12 minutes, and then to a curing treatment at 110° C. for4 hours. The thus formed hard coat film has an index of refraction of1.58, pencil hardness of 8H and a thickness of 2.8 μm.

The thus obtained cured lens was subjected to a pretreatment using asurface treatment plasma-generating apparatus (PR501A, commerciallyavailable from Yamato Kagaku Co., Japan) at an oxygen flow of 100ml/min. and at an output power of 50W for 1 minute.

Then the coating composition obtained in (3) (b) was applied on thepretreated hard coat film by spin coating with a rotation speed of 3,500rpm and a rotation time of 30 seconds. After the spin coating, thecoated composition was subjected to a preliminary curing at 82° C. for12 minutes and then to a curing treatment at 93° C. for 4 hours to forma fluorine-containing polyorganosiloxane film. The thus formed film hasa thickness of 100 nm and a index of refraction of 1.39.

The total light transmittance of the thus prepared optical article was96.1%.

For comparision, an optical article was prepared in the same mannerexcept that the hard coat film was omitted.

The obtained optical articles were tested for their properties asdescribed in (5) below. The results are shown in the following Table 1.

                  TABLE 1                                                         ______________________________________                                                       Example 1                                                                             Comparative Ex. 1                                      ______________________________________                                        Total Light Transmittance (%)                                                                  96.1      96.3                                               Dyeability (%)   40.0      90.2                                               Appearance after Dying                                                                         good      --                                                 Steel Wool Hardness                                                                            A         C                                                  ______________________________________                                    

As is seen from Table 1, the anti-reflection lens having the hard coatfilm was satisfactory in all of anti-reflection properties, dyeabilityand surface hardness, while the one having no hard coat film hadinsufficient dyeability and surface hardness and cannot be usedpractically.

(5) Testing Methods (5)-1 Dyeability

The dyeability is expressed in terms of the total light transmittance ofthe article after dipping the article in a disperse dye (mixture of 3colors of red, blue and yellow) at 93° C. for 15 minutes.

(5)-2 Appearance After Dying

Appearance was examined by gross examination with eyes.

Good: Lens was uniformly dyed.

Bad: Lens was non-uniformly dyed.

(5)-2 Steel Wool Hardness

The coating film was abraded with #0000 steel wool, and the degree ofscratching of the film wa examined by gross examination. The evaluationcriteria are as follows:

A: No scratch are given even by a strong abrasion.

B: Scratches are given by a strong abrasion.

C: Scratches are given by a weak abrasion.

EXAMPLES 2-4, Comparative Example 2

A diethyleneglycolbisallyl carbonate polymer lens (diameter of 71 mm,thickness of 2.1 mm, CR-39 Planolens, commercially available fromPittsburgh Plate Glass) having an index of refraction of 1.50 was usedas the plastic transparent substrate after dipping in aqueous sodiumhydroxide solution with a concentration of 20 wt % and washing. As acoating composition for forming the fluorine-containingorganopolysiloxane film, compositions similar to that used in Example 1but having a varying ratio (shown in Table 2) of methyltrimethoxysilaneto 3,3,3-trifluoropropyltrimethoxysilane andγ-glycidoxypropyltrimethoxysilane were used. Optical articles wereprepared in the same manner as in Example 1.

For comparison, an optical article was prepared in the same mannerexcept that the hard coat film was omitted.

The results are shown in Table 2. As is apparent from Table 2, theoptical article having no hard coat film (Comparative Example 2) hadvery low surface hardness.

                                      TABLE 2                                     __________________________________________________________________________                                        Total                                                                         Light                                            3,3,3-trifluorotri-                                                                    Methyltrimethoxy-                                                                       γ-glycidoxypropyl-                                                                Trans-                                                                             Steel                                                                              Dye-                                                                              Top Film                           methoxysilane                                                                          silane    trimethoxysilane                                                                        mittance                                                                           Wool ability                                                                           Film  Index of                     (parts by weight)                                                                      (parts by weight)                                                                       (parts by weight)                                                                       (%)  Hardness                                                                           (%) Thickness                                                                           Reflaction            __________________________________________________________________________    Example 2                                                                            50       50         0        96.4 A    40.0                                                                              100   1.39                  Example 3                                                                            41       41        18        96.6 A    35.7                                                                              110   1.40                  Example 4                                                                            65        0        35        96.1 B    15.6                                                                               90   1.38                  Comparative                                                                          50       50         0        95.4 C    45.3                                                                              100   1.39                  Example 2                                                                     __________________________________________________________________________

EXAMPLES 5 and 6

The optical articles obtained in Examples 1 and 2 were subjected to ananti-static treatment by using a surface treatment plasma-generatingapparatus (PR501A, commercially available from Yamato Kagaku Co., Japan)with 100 ml/min. of oxygen flow and with an output power of 50W for 3minutes.

The fluorine/silicon ratio (F/Si) by weight of the thus treated top filmwas 0.04/1 in the uppermost region thereof. The average fluorine/siliconratio in the entire top film was 0.08/1.

The total light transmittance of the optical article was 96.1% (Example5) and 96.4% (Example 6). In both examples, the half life of the voltageof the electric charge as determined by the method described below wasnot more than 1 second, and the punch dust was not attached at all tothe article from the begining in the punch dust test hereinafterdescribed.

For comparison, the optical articles which were not subjected to theanti-static treatment were tested for their half life of the voltage ofthe electric charge and were subjected to a punch dust test. Thefluorine/silicon ratio in the top film of the articles was 0.08/1 byweight. The half life of the voltage of the electric charge was 121seconds (untreated article of Example 5) or 360 seconds or more(untreated article of Example 6), and the results of the punch dust testwere 20 and 30, respectively. Thus, the untreated optical articles werelikely to be charged.

The methods of determining the half life and conducting the punch dusttest were as follows:

(A) Half Life of Voltage of Electric Charge

Using a static honest meter, the articles were charged at 10 kV, 1000rpm at 20° C., 65% RH, and then the half life of the voltage of theelectric charge was determined.

(B) Punch Dust Test

At 20°-25° C., 50-70% RH, the optical articles were wiped with a skin ofdeer to electrically charge the articles. On the other hand, punch dustwas scattered on a desk. The charged optical article was brought toclose to the punch dust to a distance of 1-2 cm from the dust. Theoptical article was fixed in the same position for 30 minutes, and thenumber of dust retained by the article without falling down was counted.

EXAMPLE 7 (1) Preparation of Fluorine-Containing Composition

(a) Preparation of Hydrolysate

To a reactor with a rotating member of a magnetic stirrer, 5.2 g ofγ-glycidoxypropyltrimethoxysilane and 3.1 g of3,3,3-trifluoropropyltrimethoxysilane were fed. While keeping thetemperature of the liquid at 30° C. and stirring the liquid with themagnetic stirrer, 2.8 g of 0.01 N aqueous hydrochloric acid was addeddropwise. After addition of the hydrochloric acid, the mixture wasstirred for 10 minutes at room temperature to obtain a hydrolysate.

(b) Preparation of Coating Composition

To the thus obtained hydrolysate, were added 141.6 g of n-propylalcohol, 60.7 g of distilled water and 18.8 g of ethylCellosolve and themixture was stirred. To the resulting mixture, were added 16.0 g ofmethanol silica sol, 2.2 g of silicone-based surface active agent inn-propyl alcohol at a concentration of 5% by weight, and 0.6 g ofaluminum acetylacetonate. The mixture was well stirred to obtain acoating composition.

(2) Preparation of Anti-Reflection Article

An article was prepared in the same manner as in Example 1 using thesubstrate obtained in Example 1 (1) and the coating composition obtainedin Example 1 (2), and the resulting article was subjected to a plasmatreatment at 200 ml/min. of oxygen flow and at an output power of 50Wfor 1 minute.

Then the coating composition obtained in this example (1)(b) was coatedon the thus prepared article by a spin coating method employing arotation speed of 3,500 rpm and rotation time of 30 seconds. Aftercoating the composition, the article was subjected to a preliminarycuring at 82° C. for 12 minutes and then to a curing treatment at 110°C. for 4 hours to obtain an anti-reflection optical lens.

The total light transmittance of the thus obtained optical article was95.2%.

The properties of the thus formed lens were tested as in Example 1-(5).The results are as follows:

Dyeability (%): 37.0

Appearance after Dying: good

Steel Wool Hardness: A

(3) Anti-Static Treatment

The optical article obtained in (2) above was subjected to a plasmatreatment using a surface treatment plasma-generating apparatus (PR501A,commercially available from Yamato Kagaku Co., Japan) with an oxygenflow of 200 ml/min. and an output power of 50W for 30 seconds.

The total light transmittance of the thus treated article was 95.2%. Thehalf life of the voltage of the electric charge was 10 seconds or less,and no punch dust was attached to the article in the punch dust test.

The fluorine/silicon (F/Si) ratio in the uppermost region of the topfilm was 0.05/1 by weight, while the average fluorine/silicon ratio inthe entire top film was 0.07/1. The fluorine/silicon ratio in theuppermost region of the top film of the untreated article was 0.07/1 byweight.

EXAMPLE 8 (1) Preparation of Transparent Lens

A diethyleneglycolbisallyl carbonate polymer lens (diameter of 71 mm,thickness of 2.1 mm, CR-39 Planolens) with an index of refraction of1.50 was dipped in an aeuous sodium hydroxide solution of aconcentration of 20 wt % and washed. The lens was coated with thecomposition and the coating was cured as in Example 1 (4).

(2) Preparation of Anti-Reflection Optical Article

An anti-reflection optical article was prepared in the same manner as inExample 7-(2). The thus prepared article had the following properties:

Total Light Transmittance: 95.8%

Dyeability: 30%

Appearance after Dying: good

Steel Wool Hardness: A

(3) Anti-Static Treatment

The anti-reflection optical lens obtained in (2) was subjected to aplasma treatment in the same manner as in Example 7 (3).

The total light transmittance was 95.8%. The half life of the voltage ofthe electric charge was 10 seconds or less, and no punch dust wasattached to the article in the punch dust test.

The fluorine/silicon (F/Si) ratio in the uppermost region of the topfilm was 0.05/1 by weight, while the average fluorine/silicon ratio inthe entire top film was 0.07/1. The fluorine/silicon ratio in theuppermost region of the top film of the untreated article was 0.07/1 byweight.

We claim:
 1. A process for producing an anti-reflection optical articlewhich comprises:providing a transparent plastic substrate on which ahard coat film having an index of refraction of not less than 1.52 isformed; applying a liquid coating composition comprising afluorine-containing organic silicon compound and/or a hydrolysatethereof, on the hard coat film; and curing the applied composition toform a fluorine-containing organopolysiloxane-based film with an indexof refraction lower than that of the hard coat film by not less than0.02.
 2. The process of claim 1, wherein the fluorine-containing organicsilicon compound has the formula:

    (R.sup.1 Q)SiX.sub.a Y.sub.3-a                             (I)

wherein R¹ is a C₁ -C₂₀ flourine-containing alkyl group which maycontain one or more ether bonds and/or ester bonds; Q is a divalentorganic group; X is a C₁ -C₄ alkyl group; Y is a halogen, alkoxy or RCOOgroup (wherein R is a hydrogen or a C₁ -C₄ lower alkyl group); and a isan integer of 0 or
 1. 3. The process of claim 1, wherein the coatingcomposition further comprises a silica sol of a high molecular weightsilic acid in the form of a colloidal dispersion.
 4. A process forproducing an anti-reflection optical article which comprises:providing atransparent plastic substrate on which a hard coat film having an indexof refraction of not less than 1.52 is formed; applying a liquid coatingcomposition comprising a fluorine-containing organic silicon compoundand/or a hydrolysate thereof, on the hard coat film; heating the appliedcomposition to form a fluorine-containing organopolysiloxane-based filmwith an index of refraction lower than that of the hard coat film by notless than 0.02, the silicon to fluorine ratio by weight in the entirefluorine-containing organopolysiloxane-based film is 0.02 to 10, and theratio in the uppermost region or the fluorine-containingorganopolysiloxane-based film is less than 80% that of the entirefluorine-containing organopolysiloxane-based film; and subjecting thesurface of the thus formed fluorine-containing organopolysiloxane-basedfilm to an activated gas treatment.
 5. The process of claim 4, whereinthe activated gas treatment is a plasma treatment or a corona dischargetreatment.